Page last updated: 2024-10-21

urea and BCKD Deficiency

urea has been researched along with BCKD Deficiency in 12 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Research

Studies (12)

Timeframe	Studies, this research(%)	All Research%
pre-1990	9 (75.00)	18.7374
1990's	2 (16.67)	18.2507
2000's	1 (8.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Barschak, AG	1
Marchesan, C	1
Sitta, A	1
Deon, M	1
Giugliani, R	1
Wajner, M	1
Vargas, CR	1
Wellner, D	1
Meister, A	1
Morris, AA	1
Leonard, JV	2
Snyderman, SE	1
Omenn, GS	1
Dixon, MA	1
Frimpter, GW	1
Martin, JJ	2
Schlote, W	2
Hooft, C	1
Carton, D	1
Plöchl, E	1
Menkes, JH	1

Reviews

7 reviews available for urea and BCKD Deficiency

Article	Year
A survey of inborn errors of amino acid metabolism and transport in man. Annual review of biochemistry, 1981, Volume: 50 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Branched-Chain; Biological Transport	1981
Early recognition of metabolic decompensation. Archives of disease in childhood, 1997, Volume: 76, Issue:6 Topics: Biomarkers; Brain Diseases, Metabolic; Child; Fatty Acids; Glycogen Storage Disease Type I; Humans;	1997
The dietary therapy of inherited metabolic disease. Progress in food & nutrition science, 1975, Volume: 1, Issue:7-8 Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C	1975
Inborn errors of metabolism: clues to understanding human behavioral disorders. Behavior genetics, 1976, Volume: 6, Issue:3 Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter	1976
Intercurrent illness in inborn errors of intermediary metabolism. Archives of disease in childhood, 1992, Volume: 67, Issue:11 Topics: Acidosis; Child; Child, Preschool; Emergencies; Fatty Acids; Health Education; Humans; Infant; Infan	1992
Aminoacidurias due to inherited disorders of metabolism. 2. The New England journal of medicine, 1973, Oct-25, Volume: 289, Issue:17 Topics: Acidosis; Alanine; Amino Acid Metabolism, Inborn Errors; Arginase; Arginine; Carbamates; Citrulline;	1973
[Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles]. Wiener medizinische Wochenschrift (1946), 1970, Oct-10, Volume: 120, Issue:41 Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carbohydrate Met	1970

Other Studies

5 other studies available for urea and BCKD Deficiency

Article	Year
Maple syrup urine disease in treated patients: biochemical and oxidative stress profiles. Clinical biochemistry, 2008, Volume: 41, Issue:4-5 Topics: Antioxidants; Cholesterol; Cholesterol, HDL; Cholesterol, LDL; Creatine; Glucose; Humans; Hydro-Lyas	2008
Neuropathological study of aminoacidurias. Monographs in human genetics, 1972, Volume: 6 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Central Nervous System; Cystathionine; Female; Gl	1972
Pediatric clinical aspects of aminoacidopathies. Monographs in human genetics, 1972, Volume: 6 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Arginine; Child; Child, Preschool; Female; Homocy	1972
Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study. Journal of the neurological sciences, 1972, Volume: 15, Issue:1 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Central Nervous System; Chi	1972
Disorders of amino acid metabolism--1971. California medicine, 1971, Volume: 115, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease;	1971